A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993369



Internal ID21902712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40315308..40315461hg38UCSC Ensembl
chr3:40356799..40356952hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993369
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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